Advocacy International, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K874027 | LIPASE UV [TOYO] | May 27, 1988 |
| K873792 | SEPACELL R-500 AND SEPACELL R-500A | January 19, 1988 |
| K855251 | MODIFICATION ASAHI NEW PAN-SERIES HEMOFILTERS | February 4, 1986 |
| K855212 | ASAHI AM SERIES DIALYZERS | January 21, 1986 |
| K854259 | SEPACELL R-500 & SEPACELL R-500A | January 8, 1986 |
| K842103 | TOYO JOZO URIC ACID TEST | August 12, 1984 |
| K842104 | TOYO JOZO G-GTP TEST | August 10, 1984 |
| K830183 | ASAHI HOLLOW FIBER KIDNEYS NR SERIES | March 17, 1983 |
| K830231 | ASAHI HOLLOW FIBER KIDNEYS, AM-SERIES | March 17, 1983 |
| K823733 | EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR | January 14, 1983 |
| K813037 | FLOWGUARD CATHETERS & CANNALAE | December 14, 1981 |
| K813034 | POLYSTAN HEART LUNG MACHINE SYS | November 27, 1981 |
| K813035 | POLYSTAN VERTICLUDE BLOOD PUMP | November 27, 1981 |